Clinical Trial Associate

🔥 46 minutes ago

🇫🇷 France – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

✨ Clinical Trial Associate

👻 Ghost score 10%

What it means: the chance that no one is really hiring for this job.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.Why this score:

• Just posted.
• Jobs at this company usually fill in 21 days.
• No salary listed.

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ICON plc

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1990

💼 Consulting

🏥 Healthcare

📦 Logistics

Consulting • Healthcare • Logistics

ICON plc is a global provider of clinical, consulting, and commercial services across various sectors in the healthcare and pharmaceutical industries. They offer a wide range of clinical solutions, including decentralised clinical trials, cardiac safety solutions, early clinical laboratories, and medical imaging. ICON also provides technology solutions that support drug development from early phases to post-marketing. Their therapeutic expertise spans cardiovascular, oncology, internal medicine, and more, with a strong focus on transformative therapies like cell and gene therapies and biosimilars. ICON is recognized as a leading Contract Research Organisation (CRO), regularly providing thought leadership and contributing to industry publications and events. Their services are tailored to optimize clinical trials, offer regulatory intelligence, and deliver real-world evidence through robust data analysis and patient-centric solutions.

📋 Description

• Support site start-up and activation activities • Manage investigator site payments and invoicing activities • Generate Requests for Invoice (RFIs) from patient visit data extracts • Collaborate with investigator sites and CRAs to resolve payment and invoice issues • Set up and maintain site payment records in systems • Process and track site payments, ensuring accuracy and compliance • Monitor payment timelines and follow up on outstanding invoices and queries • Ensure adherence to financial processes and study-specific payment requirements • Track invoice status, monitor payment timelines, and proactively address outstanding issues

🎯 Requirements

• Bachelor's degree in life sciences or a related field • Previous experience in clinical research or regulatory affairs preferred, but not required • Strong attention to detail and organizational skills • Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams • Ability to work independently and manage multiple tasks simultaneously in a fast-paced environment • Legal right to work in the country where the role is based

🏖️ Benefits

• Competitive base salary and performance related incentives • Health and wellbeing programmes including medical, dental, and vision coverage where applicable • Retirement and pension plans • Life assurance and disability coverage • Employee assistance programmes and wellbeing resources • Learning and development opportunities through structured training and career pathways

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